The goal of the research was to take as many measures of pathology as
possible, with the expectation that the total picture will reveal some
measure of virulence from both the parasite and host perspectives.
Measuring host mortality
The most difficult data to obtain on virulence may be the most interesting:
reduction in host lifespan. Several methods were used to detect any
increase in mortality induced by Plasmodium infection in lizards.
Naturally infected fence lizards suffer two to six times higher mortality
in laboratory cages and, for all parasite species, infected animals are
more prone to attack by predators (Schall, 1996). Prevalence (percentage
infected) rises with the lizard’s age for every system studied, but
prevalence typically levels off or even drops for the oldest lizards
(Fig. 14.4). Long-term mark–recapture studies of infected fence lizards
(Bromwich and Schall, 1986; Eisen, 2000) and laboratory-held anoles
and rainbow lizards show that infections are seldom eliminated. Thus, the
dip in prevalence suggests that mortality increases for older lizards when
they are infected. Among sites at Hopland and Saba, there is a negative
relationship between maximum body size and the prevalence of malaria
infection (Fig. 14.5). Thus, lizards tend to be smaller in areas where
prevalence of the parasites is highest. Lizards typically grow throughout
298 J.J. Schall
< 80 80 90 100 110 120 > 124
Males
Females
Per cent of lizards infected
15
20
5
10
Fig. 14.4. Prevalence ofPlasmodium giganteumin rainbow lizards,Agama
agama, in Sierra Leone, West Africa. The pattern shown here is typical for lizard
malaria parasites. Prevalence increases with size (= age), as expected if lizards
seldom lose infection. Males are more often infected than females. Prevalence
drops for the oldest animals, suggesting that the parasite increases mortality for
these animals.